Claire F. Schretlen

ORCID: 0000-0002-0773-0474
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Chronic Kidney Disease and Diabetes
  • Kidney Stones and Urolithiasis Treatments
  • Renal Diseases and Glomerulopathies
  • Biomedical Research and Pathophysiology
  • Childhood Cancer Survivors' Quality of Life
  • Acute Kidney Injury Research
  • Dermatological and Skeletal Disorders
  • Foreign Body Medical Cases
  • Potassium and Related Disorders
  • Intestinal Malrotation and Obstruction Disorders
  • Trauma, Hemostasis, Coagulopathy, Resuscitation
  • Autoimmune Bullous Skin Diseases
  • Systemic Sclerosis and Related Diseases
  • Clinical Nutrition and Gastroenterology
  • Porphyrin Metabolism and Disorders
  • Renal and related cancers
  • Immunodeficiency and Autoimmune Disorders
  • Pediatric Urology and Nephrology Studies
  • Systemic Lupus Erythematosus Research
  • Urticaria and Related Conditions
  • Methemoglobinemia and Tumor Lysis Syndrome
  • Acute Lymphoblastic Leukemia research
  • Pancreatitis Pathology and Treatment
  • Metabolism and Genetic Disorders
  • Sympathectomy and Hyperhidrosis Treatments

Johns Hopkins Medicine
2022-2025

Johns Hopkins University
2022-2025

Kinetic Art & Technology (United States)
2024

West Virginia University
2020

The medical literature is scant with reports of twins diagnosed nephrotic syndrome associated genetic mutations. Mutations in the protein coding paired box gene 2 (PAX2) and non-muscle class I myosin, myosin 1E, (MYO1E) have been implicated development steroid-resistant syndrome. We describe first case, to our knowledge, concordant presentation simultaneous mutations PAX2 MYO1E.At 32 months 33 age, monochorionic, diamniotic twin girls presented Each experienced three relapses during or after...

10.5414/cncs110799 article EN Clinical Nephrology - Case Studies 2022-01-01

10.1681/asn.20233411s1460b article FR Journal of the American Society of Nephrology 2023-11-01

Journal of the American Society Nephrology 31(10S):p 126, October 2020. | DOI: 10.1681/ASN.20203110S1126b

10.1681/asn.20203110s1126b article EN Journal of the American Society of Nephrology 2020-10-01

10.1681/asn.20223311s1445d article EN Journal of the American Society of Nephrology 2022-11-01

A 32-day-old term girl is brought to the emergency department by her grandparents for ongoing emesis with feeds and weight loss. The patient’s birth history was complicated limited prenatal care, maternal substance abuse, perinatal hepatitis C exposure, a 14-day stay in NICU thrombocytopenia requiring platelet transfusion, eventual diagnosis of May-Hegglin anomaly. At hospital discharge she had normal count, tolerating 40 90 mL hydrolyzed formula every 3 hours, no issues voiding or...

10.1542/pir.2020-001966 article EN Pediatrics in Review 2021-10-01
Coming Soon ...